Jang Heeun, Sharma Alexis B, Dan Usan, Wong Jasmine H, Knight Zachary A, Garrison Jennifer L
Buck Institute for Research on Aging, Novato, CA 94945, USA.
Department of Physiology; University of California San Francisco, San Francisco, CA 94158, USA.
bioRxiv. 2024 Sep 27:2024.09.26.615271. doi: 10.1101/2024.09.26.615271.
Chronic dehydration is a leading cause of morbidity for the elderly, but how aging alters the fluid homeostasis system is not well understood. Here, we used a combination of physiologic, behavioral and circuit analyses to characterize how fluid balance is affected by aging in mice. We found that old mice have a primary defect in sensing and producing the anti-diuretic hormone vasopressin, which results in chronic dehydration. Recordings and manipulations of the thirst circuitry revealed that old mice retain the ability to sense systemic cues of dehydration but are impaired in detecting presystemic, likely oropharyngeal, cues generated during eating and drinking, resulting in disorganized drinking behavior on short timescales. Surprisingly, old mice had increased drinking and motivation after 24-hour water deprivation, indicating that aging does not result in a general impairment in the thirst circuit. These findings reveal how a homeostatic system undergoes coordinated changes during aging.
慢性脱水是老年人发病的主要原因,但衰老如何改变液体平衡系统尚不清楚。在这里,我们结合生理、行为和神经回路分析,以表征衰老如何影响小鼠的液体平衡。我们发现,老年小鼠在感知和产生抗利尿激素血管加压素方面存在原发性缺陷,这导致慢性脱水。对渴觉神经回路的记录和操作表明,老年小鼠保留了感知全身脱水信号的能力,但在检测进食和饮水过程中产生的全身前、可能是口咽的信号方面受损,导致短时间内饮水行为紊乱。令人惊讶的是,老年小鼠在24小时缺水后饮水和动机增加,表明衰老不会导致渴觉神经回路普遍受损。这些发现揭示了一个稳态系统在衰老过程中如何发生协调变化。